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Senior Clinical Research Scientist
hace 4 semanas
As a Senior Clinical Scientist at ICON, you will be part of a global team that delivers high-quality clinical research services to the pharmaceutical and biotechnology industries. Your primary responsibility will be to lead medical data review activities, ensuring the accuracy and integrity of clinical trial data.
Key Responsibilities:- Develop and implement medical data review plans to ensure compliance with regulatory requirements.
- Collaborate with cross-functional teams to identify and address data discrepancies and inconsistencies.
- Prepare and review Safety Slide Decks (SSDs) for cross-functional review, focusing on Adverse Events, Treatment Emergent Serious Adverse Events, and Adverse Events of Special Interest.
- Develop and maintain a comprehensive understanding of clinical trial protocols, including medical data review strategies and procedures.
- Provide expert guidance on data management and clinical trial setup, ensuring compliance with regulatory requirements.
- Proven experience in medical data review, clinical trials, and data management in the life sciences industry.
- Strong understanding of regulatory requirements, including GCP and ICH guidelines.
- Excellent communication and collaboration skills, with the ability to work effectively in a global team environment.
- Strong analytical and problem-solving skills, with the ability to identify and address data discrepancies and inconsistencies.
At ICON, we value diversity, inclusion, and belonging. We offer a competitive salary, a range of benefits, and opportunities for professional growth and development. If you are a motivated and experienced clinical scientist looking for a challenging and rewarding role, we encourage you to apply.
